Research Specialist II - FT - Days - MRH

What you’d do

Coordinate a multidisciplinary research team and manage patient visits and testing for clinical trials. Screen and consent patients using Good Clinical Practice, document results in EPIC, monitor treatment side effects, and handle sponsor visits, audits, and specimen shipping. Full time, days. Found on the employer's careers page on Oct 7, 2026. Apply through the link.

You’ll need

• Accredited program completion
• Foreign Medical Doctor degree or RN license
• Florida RN license or compact multistate license
• Good Clinical Practice (GCP) guidelines
• EPIC electronic medical record